品脱1
粒体自噬
生物
帕金
线粒体
细胞生物学
自噬
ATP-ADP转位酶
DNAJA3公司
转位酶
线粒体内膜
泛素连接酶
生物化学
线粒体融合
线粒体DNA
泛素
细胞凋亡
帕金森病
疾病
医学
染色体易位
病理
基因
作者
Mohamed A. Eldeeb,Armaan Fallahi,Andrea Soumbasis,Andrew N. Bayne,Jean‐François Trempe,Edward A. Fon
出处
期刊:Autophagy
[Informa]
日期:2024-04-10
卷期号:20 (8): 1903-1905
被引量:1
标识
DOI:10.1080/15548627.2024.2340399
摘要
Mutations in the PINK1 kinase cause Parkinson disease (PD) through physiological processes that are not yet fully elucidated. PINK1 kinase accumulates selectively on damaged mitochondria, where it recruits the E3 ubiquitin ligase PRKN/Parkin to mediate mitophagy. Upon mitochondrial import failure, PINK1 accumulates in association with the translocase of outer mitochondrial membrane (TOMM). However, the molecular basis of this PINK1 accumulation on the TOMM complex remain elusive. We recently demonstrated that TIMM23 (translocase of the inner mitochondrial membrane 23) is a component of the PINK1-supercomplex formed in response to mitochondrial stress. We also uncovered that PINK1 is required for the formation of this supercomplex and highlighted the biochemical regulation and significance of this supercomplex; expanding our understanding of mitochondrial quality control and PD pathogenesis.
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